Canonical Allele Identifier: CA2260085888
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584314C= , CM000679.2:g.41584314C= GRCh38
NC_000017.10:g.39740566C= , CM000679.1:g.39740566C= GRCh37
NC_000017.9:g.36994092C= NCBI36
NG_008624.1:g.7582G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.708G= MANE Select ENSP00000167586.6:p.Glu236=
ENST00000167586.6:c.708G= ENSP00000167586.6:p.Glu236=
ENST00000476662.1:n.158G=
NM_000526.4:c.708G= NP_000517.2:p.Glu236=
NM_000526.5:c.708G= MANE Select NP_000517.3:p.Glu236=
Search 100 bp 5'
Search 100 bp 3'